FDAJune 1, 2016device

PhoenixSpec Calibrator & Kit is used to calibrate the PhoenixSpec &#38 Phoenix AP Instruments. The instruments are then used to measure the turbidity of microbial suspensions equivalent to McFarland standards 0.10 to 4.50.

Official recall recorded by the U.S. Food & Drug Administration.

The hazard

BD has determined that the BBL PhoenixSpec Calibrator kits referenced in this recall from the following lots (5364776, 5345796 ) are labeled with an incorrect expiration date (year). The expiration date printed on the individual calibration tubes within the kit are correct but difficult to read on a portion of the tubes.

What to do

FDA enforcement status: Terminated

Brands named

becton dickinsonbectonbecton dickinson

Recall history

Other federal recalls tied to the same brand — a factual pattern, straight from the source data.

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